A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759814



Internal ID9981959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:30958215..31042465hg38UCSC Ensembl
Innerchr11:30979762..31064012hg19UCSC Ensembl
Innerchr11:30936338..31020588hg18UCSC Ensembl
Innerchr11:30936338..31020588hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3884251
hg1984251
hg1884251
hg1784251
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758261
SamplesNA12003
Known GenesDCDC5
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)esv2759814
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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