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Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank

ABSTRACT: Calling deletions covering the full region of 15q11.2 in the UK Biobank cohort of ~500,000 individuals and determining the region's association with cardiovascular and neurodevelopmental phenotypes

INSTRUMENT(S): Affymetrix

ORGANISM(S): Homo Sapiens

SUBMITTER: University of Manchester

PROVIDER: PRJEB35772 | EVA | 2020-02-06

REPOSITORIES: EVA

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			Action	DRS
	15q11.2_del_AF.vcf.gz	Vcf
	15q11.2_del_AF.vcf.gz.tbi	Vcf

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