<p>Frequencies (%) of copy number gain (right side of central axis, red) and copy number loss (left side of central axis, green) across the human genome are shown.</p
<p>On the left side, the number of SNPs located in each chromosomal arm is indicated, which were exp...
<p>Horizontal lines: oligonucleotide probes are shown in order from chromosomes 1 to 22. Within each...
Summary Copy number variations (CNVs) alter the transcriptional and translational levels of genes by...
<p><b>A: Percentage of copy number gains and losses in tumor samples compared with their normal corr...
<p>Number of SNPs is given for each of the chromosomes shown, according to data in dbSNP, HapMap, or...
<p>A) The histogram shows that the 73 CNVs were evenly distributed along the X chromosome but displa...
To further explore the extent of structural large-scale variation in the human genome, we assessed c...
<p>Note: 1: when two or more adjacent cytobands have copy number changes at a frequency above 30% (g...
<p>Below each bar chart of coverage values is a putative reconstruction of the copy number on each c...
<p>Frequency of chromosomal aberrations. Fraction of samples with copy number >2.8 (red bars above b...
Determining how somatic copy-number alterations (SCNAs) promote cancer is an important goal. We char...
Global patterns of Copy Number Variations (CNVs) in chromosomes are required to understand the dynam...
<p>Frequencies of gains (in red) and losses (in blue) are indicated. Vertical bars in B represent de...
a) Proportion of the genome subject to subclonal SCNAs (ASCAT median = 0.28, Refphase median = 0.25,...
<p>In brackets the proportion of samples with the CNV and the proportion of the specific type of rea...
<p>On the left side, the number of SNPs located in each chromosomal arm is indicated, which were exp...
<p>Horizontal lines: oligonucleotide probes are shown in order from chromosomes 1 to 22. Within each...
Summary Copy number variations (CNVs) alter the transcriptional and translational levels of genes by...
<p><b>A: Percentage of copy number gains and losses in tumor samples compared with their normal corr...
<p>Number of SNPs is given for each of the chromosomes shown, according to data in dbSNP, HapMap, or...
<p>A) The histogram shows that the 73 CNVs were evenly distributed along the X chromosome but displa...
To further explore the extent of structural large-scale variation in the human genome, we assessed c...
<p>Note: 1: when two or more adjacent cytobands have copy number changes at a frequency above 30% (g...
<p>Below each bar chart of coverage values is a putative reconstruction of the copy number on each c...
<p>Frequency of chromosomal aberrations. Fraction of samples with copy number >2.8 (red bars above b...
Determining how somatic copy-number alterations (SCNAs) promote cancer is an important goal. We char...
Global patterns of Copy Number Variations (CNVs) in chromosomes are required to understand the dynam...
<p>Frequencies of gains (in red) and losses (in blue) are indicated. Vertical bars in B represent de...
a) Proportion of the genome subject to subclonal SCNAs (ASCAT median = 0.28, Refphase median = 0.25,...
<p>In brackets the proportion of samples with the CNV and the proportion of the specific type of rea...
<p>On the left side, the number of SNPs located in each chromosomal arm is indicated, which were exp...
<p>Horizontal lines: oligonucleotide probes are shown in order from chromosomes 1 to 22. Within each...
Summary Copy number variations (CNVs) alter the transcriptional and translational levels of genes by...