A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv779220



Internal ID16073176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76163993..76225898hg38UCSC Ensembl
Innerchr11:75875037..75936942hg19UCSC Ensembl
Innerchr11:75552685..75614590hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3861906
hg1961906
hg1861906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555446
Supporting Variants
Samples
Known GenesWNT11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv779220
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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