- Eighteen unique cytoband regions overlapping the mGluR network with significant CNV enrichment in studied NDD cohorts 15,654 individuals (7920 ADHD, 4318 ASD, and 3416 both ADHD and ASD), as well as 19,993 controls. CNTN4 deletions are most significantly overrepresented in ADHD and all NDD cases. Four additional deletions are overrepresented in ADHD cases. 22q11.21 and 16p11.2 duplications are significantly associated in comorbid patients with ADHD and Autism. See Supplementary Tables S1 and S2 for ADHD and autism phenotype query parameters. Green-yellow–red color scale where color gradient indicates where each cell p value falls in that range. Green: non-significant, yellow: minimally significant, red: very significant. Bold indicates the most significant NDD sub-cohort for each locus. Italics indicates odds ratio < 1 control enrichment. Full result sets for each phenotype subgroup are provided in Supplementary Tables 4, 5, and 6
