Variant Details

Variant: esv2759278

Internal ID

9981423

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr4:116601155..116699723	hg38	UCSC Ensembl
Inner	chr4:117522311..117620879	hg19	UCSC Ensembl
Inner	chr4:117741759..117840327	hg18	UCSC Ensembl
Inner	chr4:117879914..117978482	hg17	UCSC Ensembl

Cytoband

4q26

Allele length

Assembly	Allele length
hg38	98569
hg19	98569
hg18	98569
hg17	98569

Variant Type

CNV gain+loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

esv2757951

Samples

NA18998, NA18502, NA19141, NA11995, NA19204, NA18861, NA18524, NA18855, NA19145, NA19092, NA07029, NA12248, NA12146, NA10857, NA07357, NA18969, NA18563, NA19127, NA19192, NA18940, NA18550, NA19201, NA18635, NA18860, NA19131, NA18571, NA12762, NA12005, NA12156, NA19207, NA19159, NA19200, NA11993, NA10847, NA19210, NA12760, NA12003, NA18529, NA18637, NA18976, NA11839, NA10838, NA18981, NA12234, NA19202, NA19142, NA11840, NA18912, NA18857, NA12239, NA19099, NA12707, NA19101, NA19132, NA18570, NA18858, NA19012, NA18974, NA18576, NA18608, NA19094, NA19003, NA18914, NA19206, NA18542, NA12716, NA18952, NA12864, NA18863, NA18564, NA19140, NA19100, NA12873, NA19144, NA18992, NA12763, NA06994, NA18971, NA19211, NA19093, NA10860, NA18609, NA18506, NA19102, NA12875, NA18854, NA19116, NA18972, NA18552, NA19129, NA18968, NA12154, NA18612, NA19153, NA18562

Known Genes

Method

BAC aCGH

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).

Platform

Agilent

Comments

Reference

Redon_et_al_2006

Pubmed ID

17122850

Accession Number(s)

esv2759278

Frequency

Sample Size	270
Observed Gain	74
Observed Loss	21
Observed Complex	0
Frequency	n/a