Figure 5
From: Copy number variation signature to predict human ancestry
Frequency of Copy Number Gains and Losses for the 73 unique caCNVs among the HapMap Training Set of A) European ancestry (CEU), B) African ancestry (YRI), and C) Han Chinese ancestry (CHB). The panel is shown in ascending order (top to bottom) by statistical significance obtained using the nearest shrunken centroid analysis. The genomic coordinates of the caCNVs are based on NCBI Build 36, UCSC Version hg18. The caCNVs that affect coding sequence are designated with (cds) following the genomic coordinates. Those caCNVs that are novel to this analysis are indicated with an asterisk after the genomic coordinates. (copy number losses: black; copy number gains: grey).