<p>A histogram of the difference in allele frequency for the non-reference allele between Hutterites and the CEU individuals from the 1000 Genomes Project is shown. On the x-axis are bins for the absolute value of the non-reference allele frequency in the Hutterites minus the allele frequency in CEU. The y-axis represents the number of CNVs in each bin.</p
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...
<p><b>(A)</b> Allele frequency spectrum of bi-allelic CNVs across all 66 individuals, showing most d...
<p>The table shows the distribution of CNV patterns among haplogroups for ten variants that showed o...
Copy number Variants (CNVs), which comprise deletions, insertions and inversions of genomic sequence...
<p>a) Percent of Global CNV load across all populations. A total of 44109 CNVs across the genome sho...
<p>Common CNV with significant difference in allele frequencies compare to the HapMap3 dataset.</p
<p>From a total of 1718 individuals, 1506 could be assigned to specific haplogroups based on a limit...
Global patterns of Copy Number Variations (CNVs) in chromosomes are required to understand the dynam...
Global patterns of copy number variations (CNVs) in chromosomes are required to understand the dynam...
Differences between genomes can be due to single nucleotide variants (SNPs), translocations, inversi...
<p>(a) represents the CNPs shared between the HapMap populations (CEU, CHB, JPT, YRI) and the Indian...
Item does not contain fulltextRecent studies have revealed a new type of variation in the human geno...
Differences between genomes can be due to single nucleotide variants (SNPs), translocations, inversi...
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...
<p><b>(A)</b> Allele frequency spectrum of bi-allelic CNVs across all 66 individuals, showing most d...
<p>The table shows the distribution of CNV patterns among haplogroups for ten variants that showed o...
Copy number Variants (CNVs), which comprise deletions, insertions and inversions of genomic sequence...
<p>a) Percent of Global CNV load across all populations. A total of 44109 CNVs across the genome sho...
<p>Common CNV with significant difference in allele frequencies compare to the HapMap3 dataset.</p
<p>From a total of 1718 individuals, 1506 could be assigned to specific haplogroups based on a limit...
Global patterns of Copy Number Variations (CNVs) in chromosomes are required to understand the dynam...
Global patterns of copy number variations (CNVs) in chromosomes are required to understand the dynam...
Differences between genomes can be due to single nucleotide variants (SNPs), translocations, inversi...
<p>(a) represents the CNPs shared between the HapMap populations (CEU, CHB, JPT, YRI) and the Indian...
Item does not contain fulltextRecent studies have revealed a new type of variation in the human geno...
Differences between genomes can be due to single nucleotide variants (SNPs), translocations, inversi...
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...