A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758259



Internal ID9980336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25612257..25821119hg38UCSC Ensembl
Innerchr11:25633803..25842666hg19UCSC Ensembl
Innerchr11:25590379..25799242hg18UCSC Ensembl
Innerchr11:25590379..25799242hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38208863
hg19208864
hg18208864
hg17208864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759811
Supporting Variantsessv12487, essv14719, essv13864, essv11214, essv16207
SamplesNA19204, NA19207, NA19159, NA19161, NA18854
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)esv2758259
Frequency
Sample Size270
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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