Variant Details

Variant: essv19042

Internal ID

9954398

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr10:46453530..46474562	hg38	UCSC Ensembl
Inner	chr10:47074891..47096230	hg19	UCSC Ensembl
Outer	chr10:46943377..47592184	hg19	UCSC Ensembl
Inner	chr10:46494897..46516236	hg18	UCSC Ensembl
Outer	chr10:46363383..47062190	hg18	UCSC Ensembl
Inner	chr10:46494897..46516236	hg17	UCSC Ensembl
Outer	chr10:46363383..47062190	hg17	UCSC Ensembl

Cytoband

10q11.22

Allele length

Assembly	Allele length
hg38	21033
hg19	648808
hg18	698808
hg17	698808

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2757382

Supporting Variants

Samples

NA07034

Known Genes

AGAP9, ANTXRLP1, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, FAM35DP, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15

Method

SNP array

Analysis

The algorithm used to call CNVs using the 500K EA platform was developed to accurately define CNV regions using a large set of reference samples and is described in detail in a separate publication (Komura 2006). The algorithm contains three major parts: 1) Intensity pre-processing using an improved version of Genomic Imbalance Map (GIM) (Ishikawa et al. 2005), including probe selection, noise reduction, normalization, and intensity ratio adjustment based on affinity differences between alleles of a SNP, 2) CNV extraction, which identifies CNVs from all pair-wise comparisons using a modified SW-ARRAY, and 3) A copy number inference step which utilizes signal ratios and SNP information to more precisely define CNV boundaries and the copy number within each region.

Platform

Affymetrix GeneChip Early Access Mapping 500K Set Array (250K_Nsp_SNP)

Comments

Reference

Redon_et_al_2006

Pubmed ID

17122850

Accession Number(s)

essv19042

Frequency

Sample Size	270
Observed Gain	1
Observed Loss	0
Observed Complex	0
Frequency	n/a