CNVs impacting NRXN1 (with ADHD, OCD, anxiety traits, ASD, executive function and learning problems), ASTN2 in male (with ADHD, anxiety and seizure) and CHD2 (ADHD, learning problems, epilepsy and hearing problems) were examples of non-recurrent clinically significant CNVs associated with phenotypes (Fig. 1C; Table 2; Supplementary Material, Table S3). The gene discussed is NRXN1; the disease is epilepsy.