A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554855



Internal ID15995578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602150..55683837hg38UCSC Ensembl
Innerchr11:55369626..55451313hg19UCSC Ensembl
Innerchr11:55126202..55207889hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3881688
hg1981688
hg1881688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n54
Supporting Variantsnssv775695, nssv775693, nssv775694
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554855
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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