A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6866953



Internal ID9917053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:41800725..41801055hg38UCSC Ensembl
Outerchr11:41822275..41822605hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744401
Supporting Variants
SamplesSSM089
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6866953
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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