Global characterization of copy number variants in epilepsy patients from whole genome sequencing
Fig 2
CNVs in the epilepsy and control cohorts.
a) Regions with a CNV in each epilepsy patient. b) Each CNV in the CNV catalog of the epilepsy and control cohorts was annotated with its maximum frequency in five CNV databases. c) Enrichment in exonic sequence for all CNVs (left) and rare CNVs (right), larger than 50 Kbp (top) or smaller than 50 Kbp (bottom). The fold-enrichment (y-axis) represents how many CNVs overlap coding sequences compared to control regions randomly distributed in the genome.