A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv771089



Internal ID16065045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38227656..38292703hg38UCSC Ensembl
Innerchr11:38249206..38314253hg19UCSC Ensembl
Innerchr11:38205782..38270829hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3865048
hg1965048
hg1865048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554032
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv771089
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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