A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778536



Internal ID16072492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66944758..66945393hg38UCSC Ensembl
Innerchr11:66712229..66712864hg19UCSC Ensembl
Innerchr11:66468805..66469440hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38636
hg19636
hg18636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555231
Supporting Variants
Samples
Known GenesPC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778536
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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