A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1916n54



Internal ID20135340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55600413..55703518hg38UCSC Ensembl
chr11:55367889..55470994hg19UCSC Ensembl
chr11:55124465..55227570hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38103106
hg19103106
hg18103106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554935, nsv554836, nsv554905, nsv554837, nsv554861, nsv554862, nsv554903, nsv554878, nsv554924
Samples1780854537_A, HGDP00189
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)dgv1916n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer