Figure 1.

Location of the 181 CNVs detected by CoDE-seq throughout the genome (from chromosome 1 to chromosomes X,Y) in the 40 participants for whom aCGH data were available. Each light grey circle depicts a participant's genome (clockwise from chromosome 1 to chromosomes X,Y). CNVs are depicted by a blue bar (copy-gain variant) or a red bar (copy-loss variant). This figure was done using the Circos software package [34].