Genome-scale copy number variant analysis in schizophrenia patients and controls from South India

RT @22Q11_Ireland: @jayjoseph22 @JonathanKaplan @CriticalMh @JDaviesPhD @wendyburn patient-specific and previously reported CNVs include de…

RT @PsychGenPapers: Genome-scale copy number variant analysis in schizophrenia patients and controls from South India https://t.co/0wXDd3Jk…

RT @22Q11_Ireland: @jayjoseph22 @JonathanKaplan @CriticalMh @JDaviesPhD @wendyburn patient-specific and previously reported CNVs include de…

@jayjoseph22 @JonathanKaplan @CriticalMh @JDaviesPhD @wendyburn patient-specific and previously reported CNVs include deletions of 11q14.1 (DLG2), 22q11.21, and 14q21.1 (LRFN5). 16p13.3 deletion (RBFOX1), 3p14.2 duplication (CADPS), and 7p11.2 duplication