Table 2 Known disease genes in the credible intervals of the seizure-associated CNV regions

From: Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

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  1. Highlighted are: (1) Darkest grey: three CNV regions with previous genome-wide statistical support for epilepsy (PMID: 32568404), (2) Medium-dark grey: six CNV regions previously implicated in epilepsy without genome-wide statistical support, (3) Medium-light grey: ten CNV regions previously reported in other neurological and psychiatric disorders, and (4) Light grey: four novel CNV regions never reported in neurological or psychiatric disorders. In the second column, DEL and DUP indicate deletions and duplications, respectively. Gene names are formatted in italic.
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