Variant Details

Variant: esv2759577

Internal ID

9981722

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr7:153696422..154114753	hg38	UCSC Ensembl
Inner	chr7:153393507..153811838	hg19	UCSC Ensembl
Inner	chr7:153024440..153442771	hg18	UCSC Ensembl
Inner	chr7:152831155..153249486	hg17	UCSC Ensembl

Cytoband

7q36.2

Allele length

Assembly	Allele length
hg38	418332
hg19	418332
hg18	418332
hg17	418332

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

esv2758142, esv2756806

Samples

NA18942, NA18991, NA18976, NA18636, NA18968, NA18623

Known Genes

DPP6

Method

BAC aCGH
SNP array

Analysis

Array images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
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)
Agilent

Comments

Reference

Redon_et_al_2006

Pubmed ID

17122850

Accession Number(s)

esv2759577

Frequency

Sample Size	270
Observed Gain	6
Observed Loss	0
Observed Complex	0
Frequency	n/a