A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12469



Internal ID9609746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:35008386..35205237hg38UCSC Ensembl
Innerchr11:35029933..35226784hg19UCSC Ensembl
Innerchr11:34986509..35183360hg18UCSC Ensembl
Innerchr11:34986509..35183360hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38196852
hg19196852
hg18196852
hg17196852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758263
Supporting Variants
SamplesNA19207
Known GenesCD44
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)essv12469
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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