A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1918n54



Internal ID20135342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55602150..55630541hg38UCSC Ensembl
chr11:55369626..55398017hg19UCSC Ensembl
chr11:55126202..55154593hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3828392
hg1928392
hg1828392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554864, nsv554881, nsv554911, nsv554879, nsv554880, nsv554912, nsv554882, nsv554884, nsv554840
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1918n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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