A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv776863



Internal ID15724133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56532454..56652553hg38UCSC Ensembl
Innerchr11:56299930..56420029hg19UCSC Ensembl
Innerchr11:56056506..56176605hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38120100
hg19120100
hg18120100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555099
Supporting Variants
Samples
Known GenesOR5AP2, OR5M1, OR5M10, OR5M11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv776863
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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