A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759812



Internal ID9981957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28902946..29050951hg38UCSC Ensembl
Innerchr11:28924493..29072498hg19UCSC Ensembl
Innerchr11:28881069..29029074hg18UCSC Ensembl
Innerchr11:28881069..29029074hg17UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38148006
hg19148006
hg18148006
hg17148006
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758260
SamplesNA18862
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)esv2759812
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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