A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418671



Internal ID15582455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94499039..94499363hg38UCSC Ensembl
Innerchr11:94232205..94232529hg19UCSC Ensembl
Innerchr11:93871853..93872177hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38325
hg19325
hg18325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819611
Supporting Variants
SamplesAK1
Known GenesANKRD49
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)nssv1418671
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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