A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553377



Internal ID15994100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6735100..6877432hg38UCSC Ensembl
Innerchr11:6756331..6898663hg19UCSC Ensembl
Innerchr11:6712907..6855239hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38142333
hg19142333
hg18142333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1626n54
Supporting Variantsnssv766334
Samples
Known GenesOR10A2, OR10A4, OR10A5, OR2AG1, OR2AG2, OR6A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553377
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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