A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1914n54



Internal ID20135338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55600413..55662960hg38UCSC Ensembl
chr11:55367889..55430436hg19UCSC Ensembl
chr11:55124465..55187012hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3862548
hg1962548
hg1862548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554866, nsv554891, nsv554908, nsv554917, nsv554892, nsv554847, nsv554830, nsv554909, nsv554829, nsv554889, nsv554848, nsv554845, nsv554893, nsv554846, nsv554849, nsv554844, nsv554827, nsv554868, nsv554918, nsv554843, nsv554869, nsv554867, nsv554927, nsv554919
Samples
Known GenesOR4C11, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1914n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss64
Observed Complex0
Frequencyn/a


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