A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29944



Internal ID11047467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600678..55683312hg38UCSC Ensembl
Innerchr11:55368154..55450788hg19UCSC Ensembl
Innerchr11:55124730..55207364hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3882635
hg1982635
hg1882635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84183
SamplesWATSON
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodOligo aCGH
AnalysisThe data were analyzed using the CGH Analytics software.
PlatformAgilent-014584 Human Genome 244K CGH Microarray (Alpha Test)
Comments
ReferenceWheeler_et_al_2008
Pubmed ID18421352
Accession Number(s)esv29944
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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