Indeed, another large-scale study (20,403 cases and 26,628 controls) analyzing the association of schizophrenia and CNVs implicated in neurodevelopmental disorders reported no statistically significant associations of 16p11.2 deletion and 15q11.2–13.1 duplication with schizophrenia and association of 2p16.3 (NRXN1) deletion with OR smaller than ten [30, 32]. The gene discussed is NRXN1; the disease is schizophrenia.