Some of the overlapping/recurrent CNVs impacted previously identified ASD genes such as DPYD, RGS7, NRXN1, CNTNAP5, ERBB4, GRM8, NRXN3, YWHAE, and DMD (Serajee et al. 2003; Wu et al. 2005; Autism Genome Project Consortium 2007; Marshall et al. 2008; Bruno et al. 2010; Pagnamenta et al. 2010; Pinto et al. 2010; Carter et al. 2011; Vaags et al. 2012), whereas others were novel, including RERE, NCKAP5, ROBO2, DAPP1, POT1, LEP, PLXNA4, CHRNB3, ZNF517, MIR3910-1/MIR3910-2, CIB2, MMP25/IL32, MYH4, RAB3A/MPV17L2, SAE1, and SYAP1 (Figures 3 and 4). The gene discussed is MIR3910-1; the disease is autism.