A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv771176



Internal ID16065132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:41552077..41807063hg38UCSC Ensembl
Innerchr11:41573627..41828613hg19UCSC Ensembl
Innerchr11:41530203..41785189hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38254987
hg19254987
hg18254987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554094
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)nssv771176
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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