These microdeletions affected 158 protein-coding RefSeq genes and exhibited an enrichment of genes previously associated with epilepsy (NRXN1, RBFOX1, PCDH7, KCNA2, EPM2A, RORB, PLCB1) and neuropsychiatric disorders (DPYD, CADM2, PARK2, GRM8, TSNARE1, TPH2, MACROD2) (Table 3). The gene discussed is RORB; the disease is epilepsy.