de novo variant associated_with Copy number variation (CNV)

Subject: de novo variant
Relation: associated_with
Object: Copy number variation (CNV)
p-value: —

Evidence from: primary | all sources

Evidence (1 sources)

CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012) PMID:22424231 cited

risk alleles arising by recent de novo mutation

confidence: 0.85