A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418963



Internal ID15582747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:118521921..118522385hg38UCSC Ensembl
Innerchr11:118392636..118393100hg19UCSC Ensembl
Innerchr11:117897846..117898310hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38465
hg19465
hg18465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819037
Supporting Variants
SamplesAK1
Known GenesKMT2A
MethodOligo aCGH
AnalysisThe array was scanned with Agilent DNA microarray scanner at 2 micron resolution. The resulting image was extracted by Agilent's Feature Extraction software. The log2 ratios were analyzed using NEXUS software. Each aberration call was manually checked to confirm the accuracy of the calls.
PlatformGSE19651
Comments
ReferenceKim_et_al_2009
Pubmed ID19587683
Accession Number(s)nssv1418963
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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