A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1909n54



Internal ID20135333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55594332..55685447hg38UCSC Ensembl
chr11:55361808..55452923hg19UCSC Ensembl
chr11:55118384..55209499hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3891116
hg1991116
hg1891116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554896, nsv554930, nsv554857, nsv554873, nsv554931, nsv554963, nsv554859, nsv554850, nsv554871, nsv554870, nsv554856, nsv554860, nsv554817, nsv554875, nsv554898, nsv554855, nsv554929, nsv554816, nsv554858, nsv554934, nsv554876, nsv554854, nsv554951, nsv554853, nsv554938, nsv554928, nsv554910, nsv554944, nsv554962, nsv554872, nsv554899, nsv554877, nsv554874, nsv554851, nsv554933, nsv554961, nsv554852, nsv554923, nsv554831, nsv554932
SamplesHGDP00637, HGDP00047, NINDS_232
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)dgv1909n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss327
Observed Complex0
Frequencyn/a


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