Variant Details

Variant: esv2759774

Internal ID

9635233

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr10:86755301..87550005	hg38	UCSC Ensembl
Inner	chr10:88515058..89309762	hg19	UCSC Ensembl
Inner	chr10:88505038..89299742	hg18	UCSC Ensembl
Inner	chr10:88505038..89299742	hg17	UCSC Ensembl

Cytoband

10q23.2

Allele length

Assembly	Allele length
hg38	794705
hg19	794705
hg18	794705
hg17	794705

Variant Type

CNV gain+loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

esv2757404, esv2758234

Samples

NA18998, NA18502, NA12717, NA19222, NA11830, NA18621, NA11829, NA19204, NA18862, NA18861, NA18508, NA12814, NA18524, NA18980, NA18855, NA12236, NA18561, NA18603, NA19092, NA18545, NA12801, NA12248, NA12146, NA12865, NA10857, NA19098, NA18870, NA12750, NA07357, NA18969, NA12813, NA18967, NA18563, NA19127, NA19192, NA19171, NA19005, NA18944, NA12812, NA19201, NA10835, NA10846, NA18995, NA10854, NA12802, NA19119, NA18635, NA18558, NA18547, NA19131, NA18960, NA18942, NA18571, NA12762, NA19138, NA18964, NA19130, NA18949, NA12761, NA12005, NA19137, NA12044, NA11994, NA19207, NA19172, NA19128, NA18966, NA19159, NA18990, NA10855, NA19209, NA10839, NA11993, NA19007, NA19210, NA12760, NA12752, NA19120, NA19194, NA12003, NA10831, NA12878, NA12872, NA19161, NA18956, NA18515, NA19205, NA18991, NA18529, NA18516, NA18637, NA18871, NA18976, NA18503, NA10838, NA18981, NA12234, NA19221, NA18573, NA11840, NA10830, NA18912, NA12892, NA19154, NA18532, NA18853, NA19099, NA12707, NA19101, NA18555, NA12144, NA06985, NA18523, NA19160, NA19132, NA10856, NA18593, NA18945, NA18974, NA18576, NA12043, NA18608, NA18953, NA19094, NA19003, NA18978, NA18914, NA18632, NA19206, NA06991, NA18961, NA18517, NA12864, NA18863, NA12057, NA10859, NA18913, NA19240, NA12873, NA10861, NA18943, NA12874, NA07348, NA18594, NA19143, NA18501, NA12740, NA18971, NA19223, NA19173, NA19211, NA18994, NA10860, NA18500, NA18609, NA18506, NA12875, NA18854, NA18872, NA18552, NA18852, NA07056, NA18505, NA19129, NA18968, NA19139, NA12006, NA07000, NA12154, NA18612, NA19153, NA18562, NA18577, NA11832, NA18620, NA18997

Known Genes

ADIRF, AGAP11, BMPR1A, FAM25A, FAM35A, GLUD1, LINC00864, LOC439994, MINPP1, MIR4678, MMRN2, NUTM2A, NUTM2A-AS1, NUTM2D, SNCG

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)

esv2759774

Frequency

Sample Size	270
Observed Gain	8
Observed Loss	173
Observed Complex	0
Frequency	n/a