A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv775962



Internal ID15723232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55625893hg38UCSC Ensembl
Innerchr11:55371021..55393369hg19UCSC Ensembl
Innerchr11:55127597..55149945hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3822349
hg1922349
hg1822349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554879
Supporting Variants
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv775962
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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