A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12606



Internal ID9972956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25170407..25343974hg38UCSC Ensembl
Innerchr11:25191953..25365520hg19UCSC Ensembl
Innerchr11:25148529..25322096hg18UCSC Ensembl
Innerchr11:25148529..25322096hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38173568
hg19173568
hg18173568
hg17173568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758258
Supporting Variants
SamplesNA19098
Known Genes
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)essv12606
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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