A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1913n54



Internal ID20135337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55600413..55650706hg38UCSC Ensembl
chr11:55367889..55418182hg19UCSC Ensembl
chr11:55124465..55174758hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3850294
hg1950294
hg1850294
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554828, nsv554890, nsv554916
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1913n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss10
Observed Complex0
Frequencyn/a


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