Variant Details

Variant: essv8660

Internal ID

9630707

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr15:30644082..30785445	hg38	UCSC Ensembl
Outer	chr15:30313633..30885273	hg38	UCSC Ensembl
Inner	chr15:30936285..31077648	hg19	UCSC Ensembl
Outer	chr15:30605836..31177476	hg19	UCSC Ensembl
Inner	chr15:28723577..28864940	hg18	UCSC Ensembl
Outer	chr15:28393128..28964768	hg18	UCSC Ensembl
Inner	chr15:28723577..28864940	hg17	UCSC Ensembl
Outer	chr15:28393128..28964768	hg17	UCSC Ensembl

Cytoband

15q13.2

Allele length

Assembly	Allele length
hg38	571641
hg19	571641
hg18	571641
hg17	571641

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2757593

Supporting Variants

Samples

NA19101

Known Genes

ARHGAP11B, CHRFAM7A, GOLGA8H, HERC2P10, LOC100288637, LOC101059918, ULK4P1, ULK4P2

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)

essv8660

Frequency

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