16p11.2 deletion risk_factor_for ASD

Subject: 16p11.2 deletion
Relation: risk_factor_for
Object: ASD
p-value: —

Evidence from: primary | all sources

Evidence (1 sources)

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011) PMID:21658581 cited

chromosome 16p11.2 deletions ... have been found in individuals with ASD

confidence: 0.95