A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758284



Internal ID9980361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97177303..97321796hg38UCSC Ensembl
Innerchr11:97048303..97192796hg19UCSC Ensembl
Innerchr11:96553513..96698006hg18UCSC Ensembl
Innerchr11:96553513..96698006hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38144494
hg19144494
hg18144494
hg17144494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759855
Supporting Variantsessv15711, essv23549
SamplesNA06993, NA18912
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)esv2758284
Frequency
Sample Size270
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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