Variant Details

Variant: esv3636227

Internal ID

6676336

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr15:40529692..40531361	hg38	UCSC Ensembl
Inner	chr15:40529703..40531350	hg38	UCSC Ensembl
Outer	chr15:40529681..40531372	hg38	UCSC Ensembl
	chr15:40821891..40823560	hg19	UCSC Ensembl
Inner	chr15:40821902..40823549	hg19	UCSC Ensembl
Outer	chr15:40821880..40823571	hg19	UCSC Ensembl

Cytoband

15q15.1

Allele length

Assembly	Allele length
hg38	1670
hg19	1670

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv15228075, essv15228027, essv15228033, essv15228105, essv15228111, essv15227985, essv15228106, essv15228039, essv15228092, essv15228089, essv15228102, essv15227988, essv15228030, essv15228066, essv15228068, essv15227996, essv15228083, essv15228082, essv15228086, essv15228029, essv15228096, essv15228008, essv15227991, essv15228097, essv15228053, essv15228026, essv15228025, essv15228005, essv15228078, essv15228043, essv15227999, essv15228048, essv15228090, essv15228063, essv15228013, essv15228085, essv15228032, essv15227987, essv15228006, essv15228001, essv15228107, essv15228034, essv15228116, essv15228018, essv15228003, essv15228072, essv15228011, essv15227998, essv15228035, essv15228012, essv15228020, essv15228057, essv15228064, essv15228101, essv15228028, essv15228080, essv15228031, essv15228047, essv15228051, essv15228049, essv15228050, essv15228000, essv15228074, essv15228058, essv15228016, essv15228054, essv15228081, essv15227992, essv15228094, essv15228087, essv15228060, essv15228046, essv15228103, essv15228109, essv15228062, essv15228095, essv15228007, essv15227997, essv15227990, essv15228009, essv15228098, essv15227994, essv15228052, essv15228055, essv15228099, essv15228010, essv15228021, essv15228017, essv15228069, essv15228073, essv15228019, essv15228110, essv15228059, essv15227995, essv15228108, essv15228002, essv15228036, essv15228067, essv15228056, essv15227986, essv15228079, essv15228038, essv15228077, essv15228070, essv15228115, essv15228093, essv15228044, essv15228114, essv15228042, essv15228040, essv15228022, essv15228004, essv15228088, essv15227989, essv15228041, essv15228014, essv15228015, essv15228024, essv15228045, essv15227993, essv15228100, essv15228084, essv15228113, essv15228071, essv15228076, essv15228037, essv15228061, essv15228023, essv15228065, essv15228104, essv15228112, essv15228091

Samples

HG03864, NA20511, HG03690, NA20882, HG03593, HG03652, NA19794, HG03965, HG01610, HG02298, HG02648, HG01586, HG03767, HG02150, HG02275, HG00306, HG00233, HG00244, HG04094, NA12751, HG02476, NA12004, HG00737, HG00341, HG02688, HG01051, HG03944, HG03680, HG03837, HG00356, HG03706, HG03943, NA20890, HG03976, HG01168, HG03765, HG04144, NA19649, HG02655, HG00355, HG00311, NA12282, HG04214, HG03910, HG03897, HG01067, HG00379, HG02490, NA19731, HG03691, HG03624, HG01973, HG03814, NA20889, NA20811, HG00338, HG02260, HG03649, HG00253, HG03862, HG01164, HG01136, NA19657, HG01171, HG03714, NA20885, NA20521, HG04107, NA20760, HG01612, HG01088, HG00132, HG03711, HG02102, NA19776, HG01092, NA20525, HG01311, NA20867, HG00273, HG03871, NA20903, HG00250, HG02494, HG00350, HG03802, HG04173, HG02649, NA06989, HG00157, HG01474, HG03006, HG01403, NA19756, HG01697, HG01589, NA20765, HG02660, NA21113, HG03848, NA11881, HG00336, HG01954, NA19735, HG02696, HG02790, HG00278, HG01939, HG03850, HG03869, HG02685, NA19783, NA12347, HG01991, HG00381, HG01935, NA20510, HG04209, HG00310, HG02239, HG02291, HG03925, HG02774, HG03922, NA19755, NA19758, HG00345, HG03890, HG01566, NA21104, HG03686, HG00362

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3636227

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	132
Observed Complex	0
Frequency	n/a