Table 1.

Genome-wide significantly associated CNV regions and credible intervals

Column 1: Cytoband localization of the CNV. Column 2: CNV type, either deletion (DEL, white background row) or duplication (DUP, grey background row). Columns 3 and 4: Genomic coordinates (in Mb) on the GRCh37 reference genome of the start and end position of the merged CNV region that is supported by genome-wide association signals. Columns 5 and 6: Lowest P-values in each CNV region and corresponding odds ratios (OR) (with 95% confidence interval) of the genome-wide CNV meta-analysis in 25,345 individuals with seizures and 492,324 controls. Column 7: GRCh37 coordinates of the credible interval(s) that contained the causal element(s) with 95% confidence. Column 8: Number of neuropsychiatric disorders that also show a significant genome-wide CNV-association in this locus. Column 9: Highest odds ratio for each locus in any of the 23 cross-disorder meta-analyses.