<p>Chromosomes and -log p-values of CNVR association with BAVM are shown on the x and the y axes; respectively. The red horizontal line corresponds to the genome wide significance threshold corrected for multiple testing using the Bonferroni procedure. <b>a</b>. Duplications using PennCNV, <b>b</b>. Deletions using PennCNV, <b>c</b>. Duplications using Birdsuite. <b>d</b>. Deletions using Birdsuite.</p
<p>This table shows significant SNP-CNV pairs found in high LD. N stands for the number of CNV micro...
<p>Shown on the x-axis are middle points of chromosomal start and end positions (NCBI Build 37) of 9...
<p>A. Manhattan plot of −log<sub>10</sub> of raw p-values by chromosome. The p<sub>genome</sub> valu...
*<p>One-sided Fisher's exact p value.</p>**<p>P value Bonferroni-adjusted for 1126 genes overlapping...
<p>The number of CNVs that overlap at least one segmental duplication was calculated for a range of ...
<p>N<sub>CNVR</sub> refers to the number of CNV loci selected from each study. Coverage with at leas...
<p>LRR values of controls and individuals with CNV for particular SNPs were extracted to check CNV c...
<p>CNV identification is based principally on quantitative analysis of the intensity of the hybridiz...
<p>The SNPs consist of both Illumina 610K chip and imputed HapMap SNPs. All CNPs and SNPs are plotte...
<p>(<b>A</b>) Association between dS of LSD pairs and CNV regions, where dS is a proxy for age since...
<p>The last column lists the genes for which at least one exon overlaps the defined CNV region. P-va...
<p>Manhattan Plot of SNP based CNV Statistics. (A)Deletions and (B)Duplications.</p
<p>Detailed view of the duplications in chromosome 12 for MefEnz. <b>A</b>. The green areas indicate...
<p>A) Genome-wide (left) and chromosome-view (right) of allele specific copy number, BAF and depth r...
<p>95,499 variants were investigated for association with DCM by logistic regression analysis. Assoc...
<p>This table shows significant SNP-CNV pairs found in high LD. N stands for the number of CNV micro...
<p>Shown on the x-axis are middle points of chromosomal start and end positions (NCBI Build 37) of 9...
<p>A. Manhattan plot of −log<sub>10</sub> of raw p-values by chromosome. The p<sub>genome</sub> valu...
*<p>One-sided Fisher's exact p value.</p>**<p>P value Bonferroni-adjusted for 1126 genes overlapping...
<p>The number of CNVs that overlap at least one segmental duplication was calculated for a range of ...
<p>N<sub>CNVR</sub> refers to the number of CNV loci selected from each study. Coverage with at leas...
<p>LRR values of controls and individuals with CNV for particular SNPs were extracted to check CNV c...
<p>CNV identification is based principally on quantitative analysis of the intensity of the hybridiz...
<p>The SNPs consist of both Illumina 610K chip and imputed HapMap SNPs. All CNPs and SNPs are plotte...
<p>(<b>A</b>) Association between dS of LSD pairs and CNV regions, where dS is a proxy for age since...
<p>The last column lists the genes for which at least one exon overlaps the defined CNV region. P-va...
<p>Manhattan Plot of SNP based CNV Statistics. (A)Deletions and (B)Duplications.</p
<p>Detailed view of the duplications in chromosome 12 for MefEnz. <b>A</b>. The green areas indicate...
<p>A) Genome-wide (left) and chromosome-view (right) of allele specific copy number, BAF and depth r...
<p>95,499 variants were investigated for association with DCM by logistic regression analysis. Assoc...
<p>This table shows significant SNP-CNV pairs found in high LD. N stands for the number of CNV micro...
<p>Shown on the x-axis are middle points of chromosomal start and end positions (NCBI Build 37) of 9...
<p>A. Manhattan plot of −log<sub>10</sub> of raw p-values by chromosome. The p<sub>genome</sub> valu...