Location of CNV Regions,
burden of rare CNVs,
and disease genes. CNV regions are shown as red and green lines (green: heterozygous duplication, dark green: homozygous duplication, red: heterozygous deletion, dark red: homozygous deletion). Stacked histogram bars represent the location of specific rare CNVs, and the number, split by phenotype (green background: duplications, red background: deletions; dark grey: bipolar, mid-grey: unknown, light grey: unaffected). Inner line plot (blue) shows location and number of disease genes. Genes of interest are labeled around the outside of the plot.