A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv774007



Internal ID16067963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50504005..50791553hg38UCSC Ensembl
Innerchr11:50463176..50750724hg19UCSC Ensembl
Innerchr11:50419752..50707300hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38287549
hg19287549
hg18287549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554417
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)nssv774007
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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