A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15711



Internal ID9968318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97031969..97200088hg38UCSC Ensembl
Innerchr11:96902969..97071088hg19UCSC Ensembl
Innerchr11:96408179..96576298hg18UCSC Ensembl
Innerchr11:96408179..96576298hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38168120
hg19168120
hg18168120
hg17168120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758283, esv2758284
Supporting Variants
SamplesNA18912
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)essv15711
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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