Comparisons of the frequency of rare copy number changes in autosomal chromosomes >100kb detected in the patient cohort and in the cohort of 500 controls.

Summary of copy number variations detected in 95 fetuses with congenital malformations.

Clara Serra-Juhé (131897)
Benjamín Rodríguez-Santiago (40878)
Ivon Cuscó (91141)
Teresa Vendrell (131903)
Núria Camats (131906)
Núria Torán (131909)
Luis A. Pérez-Jurado (131912)

October 2012

Control frequency refers to the frequency of the same type of rearrangement found in the fetus, d...

Distribution of CNV load and size across populations.

Avinash M. Veerappa (429989)
Sangeetha Vishweswaraiah (429990)
Kusuma Lingaiah (429991)
Megha Murthy (429992)
Raviraj V. Suresh (529202)
Dinesh S. Manjegowda (429993)
Nallur B. Ramachandra (429995)

April 2015

a) Percent of Global CNV load across all populations. A total of 44109 CNVs across the genome sho...

CNV burden analysis of large (>100 kb) CNVs on gonosomes and autosomes in the sporadic CoA cohort.

Julia Moosmann (740627)
Steffen Uebe (390051)
Sven Dittrich (740628)
André Rüffer (740629)
Arif B. Ekici (146432)
Okan Toka (740630)

May 2015

Total number of CNVs on gonosomes and autosomes. CNV burden was significantly higher for large (>...

Comparisons of rare copy number changes >100 kb detected in the fetuses with congenital malformations and controls.

Clara Serra-Juhé (131897)
Benjamín Rodríguez-Santiago (40878)
Ivon Cuscó (91141)
Teresa Vendrell (131903)
Núria Camats (131906)
Núria Torán (131909)
Luis A. Pérez-Jurado (131912)

October 2012

In brackets the proportion of samples with the CNV and the proportion of the specific type of rea...

Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array

de Ståhl, Teresita Díaz
Sandgren, Johanna
Piotrowski, Arkadiusz
Nord, Helena
Andersson, Robin
Menzel, Uwe
Bogdan, Adam
Thuresson, Ann-Charlotte
Poplawski, Andrzej
von Tell, Desiree
Hansson, Caisa M.
Elshafie, Amir I.
ElGhazali, Gehad
Imreh, Stephan
Nordenskjöld, Magnus
Upadhyaya, Meena
Komorowski, Jan
Bruder, Carl E.G.
Dumanski, Jan P.

March 2008

To further explore the extent of structural large-scale variation in the human genome, we assessed c...

The overall frequency of genomic copy number alterations (CNA) differs among cancer types.

Nitin Kumar (103133)
Haoyang Cai (142583)
Christian von Mering (5537)
Michael Baudis (39943)

August 2012

Boxplots show the CNA frequency distributions among tumor samples in 10 randomly selected cancer ...

Copy number variation (CNV) in relation to clinical outcome.

Marianne Berg (237475)
Oddmund Nordgaard (724888)
Hartwig Kørner (724889)
Satu Oltedal (724890)
Rune Smaaland (409701)
Jon Arne Søreide (724891)
Kjetil Søreide (511559)

April 2015

(A) Boxplot showing the number of aberrant genes in deceased patients (right) and survivors (left...

Figure 1

Rani E. George (24532)
Edward F. Attiyeh (24533)
Shuli Li (24534)
Lisa A. Moreau (24535)
Donna Neuberg (24536)
Cheng Li (6339)
Edward A. Fox (24537)
Matthew Meyerson (24538)
Lisa Diller (24539)
Paolo Fortina (24540)
A. Thomas Look (24541)
John M. Maris (24542)

February 2013

Frequency of chromosomal aberrations. Fraction of samples with copy number >2.8 (red bars above b...

Overall comparisons of autosomal CNVs observed across the case and control populations after filtering are shown in the panels above.

Rakesh Chettier (73475)
Kenneth Ward (385381)
Hans M. Albertsen (385379)

August 2014

The data represented here reflect samples with CNV-count ≥1 after outlier-removal (cases = 1,750,...

Frequency of copy number variants involving the sex chromosomes in a clinical setting

Vara, Autumn

May 2020

Copy number variants (CNVs) are a common finding in the clinical setting and contribute to both gene...

Amount of copy number (CN)-altered genome and frequency of recurrent CN-altered genes.

Ingrid Medina-Martinez (180116)
Valeria Barrón (180126)
Edgar Roman-Bassaure (570297)
Eligia Juárez-Torres (180121)
Mariano Guardado-Estrada (180155)
Ana María Espinosa (280116)
Miriam Bermudez (5659276)
Fernando Fernández (2675554)
Carlos Venegas-Vega (180152)
Lorena Orozco (180145)
Edgar Zenteno (570298)
Susana Kofman (180158)
Jaime Berumen (180161)

May 2014

Panel A shows box plots with the distribution of tumors (n = 31) according to the percentage of t...

Copy Number Variation.

Macé, A.
Kutalik, Z.
Valsesia, A.

January 2018

Differences between genomes can be due to single nucleotide variants (SNPs), translocations, inversi...

Variation of CNV distribution in five different ethnic populations.

White, S.J.
Vissers, L.E.L.M.
Geurts van Kessel, A.H.M.
Menezes, R.X. de
Kalay, E.
Lehesjoki, A.E.
Giordano, P.C.
Vosse, E. van de
Breuning, M.H.
Brunner, H.G.
Dunnen, J.T. den
Veltman, J.A.

January 2007

Item does not contain fulltextRecent studies have revealed a new type of variation in the human geno...

Net copy number changes.

Hisham Eldai (478303)
Sathish Periyasamy (478304)
Saeed Al Qarni (478305)
Maha Al Rodayyan (478306)
Sabeena Muhammed Mustafa (478307)
Ahmad Deeb (478308)
Ebthehal Al Sheikh (478309)
Mohammed Afzal Khan (478310)
Mishal Johani (478311)
Zeyad Yousef (478312)
Mohammad Azhar Aziz (478313)

October 2013

A: Percentage of copy number gains and losses in tumor samples compared with their normal corr...

Copy Number Variants in the human genome and their association with quantitative traits

Porteous, David
Campbell, Harry
Chen, Wanting

January 2011

Copy number Variants (CNVs), which comprise deletions, insertions and inversions of genomic sequence...

Summary of copy number variations detected in 95 fetuses with congenital malformations.

Clara Serra-Juhé (131897)
Benjamín Rodríguez-Santiago (40878)
Ivon Cuscó (91141)
Teresa Vendrell (131903)
Núria Camats (131906)
Núria Torán (131909)
Luis A. Pérez-Jurado (131912)

October 2012

Control frequency refers to the frequency of the same type of rearrangement found in the fetus, d...

Distribution of CNV load and size across populations.

Avinash M. Veerappa (429989)
Sangeetha Vishweswaraiah (429990)
Kusuma Lingaiah (429991)
Megha Murthy (429992)
Raviraj V. Suresh (529202)
Dinesh S. Manjegowda (429993)
Nallur B. Ramachandra (429995)

April 2015

a) Percent of Global CNV load across all populations. A total of 44109 CNVs across the genome sho...

CNV burden analysis of large (>100 kb) CNVs on gonosomes and autosomes in the sporadic CoA cohort.

Julia Moosmann (740627)
Steffen Uebe (390051)
Sven Dittrich (740628)
André Rüffer (740629)
Arif B. Ekici (146432)
Okan Toka (740630)

May 2015

Total number of CNVs on gonosomes and autosomes. CNV burden was significantly higher for large (>...

Comparisons of rare copy number changes >100 kb detected in the fetuses with congenital malformations and controls.

Clara Serra-Juhé (131897)
Benjamín Rodríguez-Santiago (40878)
Ivon Cuscó (91141)
Teresa Vendrell (131903)
Núria Camats (131906)
Núria Torán (131909)
Luis A. Pérez-Jurado (131912)

October 2012

In brackets the proportion of samples with the CNV and the proportion of the specific type of rea...

Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array

de Ståhl, Teresita Díaz
Sandgren, Johanna
Piotrowski, Arkadiusz
Nord, Helena
Andersson, Robin
Menzel, Uwe
Bogdan, Adam
Thuresson, Ann-Charlotte
Poplawski, Andrzej
von Tell, Desiree
Hansson, Caisa M.
Elshafie, Amir I.
ElGhazali, Gehad
Imreh, Stephan
Nordenskjöld, Magnus
Upadhyaya, Meena
Komorowski, Jan
Bruder, Carl E.G.
Dumanski, Jan P.

March 2008

To further explore the extent of structural large-scale variation in the human genome, we assessed c...

The overall frequency of genomic copy number alterations (CNA) differs among cancer types.

Nitin Kumar (103133)
Haoyang Cai (142583)
Christian von Mering (5537)
Michael Baudis (39943)

August 2012

Boxplots show the CNA frequency distributions among tumor samples in 10 randomly selected cancer ...

Copy number variation (CNV) in relation to clinical outcome.

Marianne Berg (237475)
Oddmund Nordgaard (724888)
Hartwig Kørner (724889)
Satu Oltedal (724890)
Rune Smaaland (409701)
Jon Arne Søreide (724891)
Kjetil Søreide (511559)

April 2015

(A) Boxplot showing the number of aberrant genes in deceased patients (right) and survivors (left...

Figure 1

Rani E. George (24532)
Edward F. Attiyeh (24533)
Shuli Li (24534)
Lisa A. Moreau (24535)
Donna Neuberg (24536)
Cheng Li (6339)
Edward A. Fox (24537)
Matthew Meyerson (24538)
Lisa Diller (24539)
Paolo Fortina (24540)
A. Thomas Look (24541)
John M. Maris (24542)

February 2013

Frequency of chromosomal aberrations. Fraction of samples with copy number >2.8 (red bars above b...

Overall comparisons of autosomal CNVs observed across the case and control populations after filtering are shown in the panels above.

Rakesh Chettier (73475)
Kenneth Ward (385381)
Hans M. Albertsen (385379)

August 2014

The data represented here reflect samples with CNV-count ≥1 after outlier-removal (cases = 1,750,...

Frequency of copy number variants involving the sex chromosomes in a clinical setting

Vara, Autumn

May 2020

Copy number variants (CNVs) are a common finding in the clinical setting and contribute to both gene...

Amount of copy number (CN)-altered genome and frequency of recurrent CN-altered genes.

Ingrid Medina-Martinez (180116)
Valeria Barrón (180126)
Edgar Roman-Bassaure (570297)
Eligia Juárez-Torres (180121)
Mariano Guardado-Estrada (180155)
Ana María Espinosa (280116)
Miriam Bermudez (5659276)
Fernando Fernández (2675554)
Carlos Venegas-Vega (180152)
Lorena Orozco (180145)
Edgar Zenteno (570298)
Susana Kofman (180158)
Jaime Berumen (180161)

May 2014

Panel A shows box plots with the distribution of tumors (n = 31) according to the percentage of t...

Copy Number Variation.

Macé, A.
Kutalik, Z.
Valsesia, A.

January 2018

Differences between genomes can be due to single nucleotide variants (SNPs), translocations, inversi...

Variation of CNV distribution in five different ethnic populations.

White, S.J.
Vissers, L.E.L.M.
Geurts van Kessel, A.H.M.
Menezes, R.X. de
Kalay, E.
Lehesjoki, A.E.
Giordano, P.C.
Vosse, E. van de
Breuning, M.H.
Brunner, H.G.
Dunnen, J.T. den
Veltman, J.A.

January 2007

Item does not contain fulltextRecent studies have revealed a new type of variation in the human geno...

Net copy number changes.

Hisham Eldai (478303)
Sathish Periyasamy (478304)
Saeed Al Qarni (478305)
Maha Al Rodayyan (478306)
Sabeena Muhammed Mustafa (478307)
Ahmad Deeb (478308)
Ebthehal Al Sheikh (478309)
Mohammed Afzal Khan (478310)
Mishal Johani (478311)
Zeyad Yousef (478312)
Mohammad Azhar Aziz (478313)

October 2013

A: Percentage of copy number gains and losses in tumor samples compared with their normal corr...

Copy Number Variants in the human genome and their association with quantitative traits

Porteous, David
Campbell, Harry
Chen, Wanting

January 2011

Copy number Variants (CNVs), which comprise deletions, insertions and inversions of genomic sequence...

Summary of copy number variations detected in 95 fetuses with congenital malformations.

Clara Serra-Juhé (131897)
Benjamín Rodríguez-Santiago (40878)
Ivon Cuscó (91141)
Teresa Vendrell (131903)
Núria Camats (131906)
Núria Torán (131909)
Luis A. Pérez-Jurado (131912)

October 2012

Control frequency refers to the frequency of the same type of rearrangement found in the fetus, d...

Distribution of CNV load and size across populations.

Avinash M. Veerappa (429989)
Sangeetha Vishweswaraiah (429990)
Kusuma Lingaiah (429991)
Megha Murthy (429992)
Raviraj V. Suresh (529202)
Dinesh S. Manjegowda (429993)
Nallur B. Ramachandra (429995)

April 2015

a) Percent of Global CNV load across all populations. A total of 44109 CNVs across the genome sho...

CNV burden analysis of large (>100 kb) CNVs on gonosomes and autosomes in the sporadic CoA cohort.

Julia Moosmann (740627)
Steffen Uebe (390051)
Sven Dittrich (740628)
André Rüffer (740629)
Arif B. Ekici (146432)
Okan Toka (740630)

May 2015

Total number of CNVs on gonosomes and autosomes. CNV burden was significantly higher for large (>...

Comparisons of the frequency of rare copy number changes in autosomal chromosomes >100kb detected in the patient cohort and in the cohort of 500 controls.

Abstract

Extracted data

Comparisons of the frequency of rare copy number changes in autosomal chromosomes >100kb detected in the patient cohort and in the cohort of 500 controls.

Abstract

Extracted data

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