A curated catalogue of human genomic structural variation




Variant Details

Variant: essv18312



Internal ID9955577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46812527..47792476hg19UCSC Ensembl
Innerchr10:46232533..47262482hg18UCSC Ensembl
Innerchr10:46232533..47262482hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19979950
hg181029950
hg171029950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758217
Supporting Variants
SamplesNA10846
Known GenesAGAP9, ANTXRL, ANTXRLP1, ANXA8, ANXA8L1, ANXA8L2, BMS1P2, BMS1P6, FAM25B, FAM25C, FAM25G, FAM35BP, FAM35DP, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
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)essv18312
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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