A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15337



Internal ID9612933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5709147..5949487hg38UCSC Ensembl
Innerchr11:5730377..5970717hg19UCSC Ensembl
Innerchr11:5686953..5927293hg18UCSC Ensembl
Innerchr11:5686953..5927293hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38240341
hg19240341
hg18240341
hg17240341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758255
Supporting Variants
SamplesNA18862
Known GenesOR52E4, OR52E6, OR52E8, OR52N1, OR52N2, OR52N4, OR52N5, OR56A3, OR56B1, TRIM22
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)essv15337
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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