A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554836



Internal ID16342245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600413..55693312hg38UCSC Ensembl
Innerchr11:55367889..55460788hg19UCSC Ensembl
Innerchr11:55124465..55217364hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3892900
hg1992900
hg1892900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1916n54
Supporting Variantsnssv775648, nssv775652, nssv775649, nssv775650, nssv775653, nssv775651
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)nsv554836
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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