A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv771183



Internal ID16065139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:41784151..41797430hg38UCSC Ensembl
Innerchr11:41805701..41818980hg19UCSC Ensembl
Innerchr11:41762277..41775556hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3813280
hg1913280
hg1813280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554100
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)nssv771183
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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