A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758278



Internal ID9980355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81699742..82119580hg38UCSC Ensembl
Innerchr11:81410784..81830622hg19UCSC Ensembl
Innerchr11:81088432..81508270hg18UCSC Ensembl
Innerchr11:81088432..81508270hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38419839
hg19419839
hg18419839
hg17419839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759843
Supporting Variantsessv23810, essv17596
SamplesNA12753, NA12763
Known GenesMIR4300
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)esv2758278
Frequency
Sample Size270
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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