A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8806



Internal ID15846718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:34199007..34204822hg38UCSC Ensembl
Outerchr11:34220554..34226369hg19UCSC Ensembl
Outerchr11:34177130..34182945hg18UCSC Ensembl
Outerchr11:34177130..34182945hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385816
hg195816
hg185816
hg175816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv20155
SamplesNA18980
Known GenesABTB2
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nsv8806
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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