Finally, we identified ten specific loci that were significantly enriched for rare SVs beyond genome-wide expectations (Additional file 2: Supplemental Results 3, Figure S6 and Tables S4–5), five of which involved genes with evidence for roles in a broad spectrum of neurological disorders (PARK2, IMMP2L, CTNNA3, CYFIP1, PTPRT) [32, 71–75]. This evidence concerns the gene CTNNA3 and nervous system disorder.