A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv774767



Internal ID15722037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54928232..55344108hg38UCSC Ensembl
Innerchr11:54695707..55111584hg19UCSC Ensembl
Innerchr11:54452283..54868160hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38415877
hg19415878
hg18415878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554618
Supporting Variants
Samples
Known GenesOR4A16, TRIM48, TRIM51HP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv774767
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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