Figure 2

Pooled capture SNV minor allele frequency correlation. Correlation plot comparing a total of 499 positions that overlapped between the custom hybridization targeted regions and the Illumina Omni-2.5-8 genome wide SNV array with at least one variant called by the array or pooled analysis. Of these 499 positions, 477 (95.6%) had at least one variant allele call by both SPLINTER and the array, 20 were called as SNVs by SPLINTER but not by the array, and 2 were called as SNVs by the array but not by SPLINTER.