Skip to main content
Figure 3 | BMC Genomics

Figure 3

From: Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization

Figure 3

P-value distribution of apparent CNVs detected by SMD in 462 samples from 154 ID trios. Data are from the analysis performed by 500 K GeneChip® AGH. Some of these apparent CNVs were merged into larger CNVs at a later stage of the analysis, but most represent individual aberrations. Apparent CNVs with p-values less than 1 × 10-8 were analysed further to determine if they were inherited or had occurred de novo. 4577 apparent CNVs were found with p-values below this threshold (shown in blue in the figure). The bin plotted at 10-17 actually contains all CNVs with p < 10-16, which is the lower limit of the tables used to calculate p-values.

Back to article page

BMC Genomics

ISSN: 1471-2164

Contact us