Variant Details

Variant: esv3603014

Internal ID

6990046

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr4:165045951..165046511	hg38	UCSC Ensembl
Inner	chr4:165045951..165046511	hg38	UCSC Ensembl
Outer	chr4:165045815..165046771	hg38	UCSC Ensembl
	chr4:165967103..165967663	hg19	UCSC Ensembl
Inner	chr4:165967103..165967663	hg19	UCSC Ensembl
Outer	chr4:165966967..165967923	hg19	UCSC Ensembl

Cytoband

4q32.3

Allele length

Assembly	Allele length
hg38	561
hg19	561

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv11678026, essv11678081, essv11678023, essv11678107, essv11678099, essv11678033, essv11678068, essv11678054, essv11678055, essv11678062, essv11678059, essv11678017, essv11678121, essv11678016, essv11678123, essv11678132, essv11678044, essv11678038, essv11678122, essv11678037, essv11678012, essv11678061, essv11678087, essv11678131, essv11678096, essv11678119, essv11678076, essv11678066, essv11678010, essv11678018, essv11678129, essv11678041, essv11678093, essv11678086, essv11678078, essv11678067, essv11678112, essv11678021, essv11678113, essv11678043, essv11678031, essv11678117, essv11678072, essv11678126, essv11678071, essv11678022, essv11678057, essv11678083, essv11678050, essv11678020, essv11678128, essv11678102, essv11678130, essv11678051, essv11678140, essv11678125, essv11678042, essv11678082, essv11678094, essv11678073, essv11678080, essv11678064, essv11678049, essv11678075, essv11678139, essv11678104, essv11678029, essv11678109, essv11678137, essv11678090, essv11678034, essv11678015, essv11678115, essv11678088, essv11678025, essv11678116, essv11678011, essv11678124, essv11678019, essv11678143, essv11678142, essv11678058, essv11678089, essv11678118, essv11678047, essv11678053, essv11678013, essv11678141, essv11678097, essv11678084, essv11678098, essv11678103, essv11678100, essv11678030, essv11678114, essv11678108, essv11678070, essv11678085, essv11678040, essv11678101, essv11678036, essv11678120, essv11678052, essv11678028, essv11678039, essv11678105, essv11678035, essv11678014, essv11678092, essv11678074, essv11678063, essv11678136, essv11678069, essv11678060, essv11678079, essv11678056, essv11678135, essv11678095, essv11678106, essv11678027, essv11678110, essv11678133, essv11678134, essv11678045, essv11678091, essv11678065, essv11678077, essv11678024, essv11678127, essv11678111, essv11678138, essv11678144, essv11678046, essv11678032, essv11678009, essv11678048

Samples

HG01986, NA18502, HG02339, NA20339, HG03366, HG02944, HG02496, HG02481, NA18861, NA19332, HG03517, NA18507, HG02318, HG02836, NA19092, NA20298, NA18878, HG03126, HG03172, HG02589, NA18870, NA19920, NA19107, HG03082, NA18519, NA19201, HG02811, HG02810, NA19448, NA19307, HG02325, NA19198, HG03485, NA18916, HG03342, HG03105, HG03578, NA19384, HG02816, HG02981, HG02562, HG02561, NA18874, HG02573, NA19917, NA19317, HG03352, NA19036, NA19901, NA19189, HG02946, HG03073, NA19209, NA19025, NA18908, HG03394, HG03114, HG02715, HG03270, HG02479, HG02943, NA19210, NA19437, HG03132, HG02582, HG01879, NA18516, HG02144, HG02953, HG01989, HG03575, NA18871, HG02508, HG01323, HG03294, HG03311, NA20299, HG03397, NA19031, NA18856, NA18853, NA19257, NA19225, NA19395, HG02594, HG01988, NA19436, NA20296, HG02330, NA19309, NA18909, NA19321, NA19256, HG02759, NA19473, NA19435, HG03117, HG01272, HG02923, NA18865, NA19835, HG03304, HG02317, HG03103, NA19323, NA19143, NA19328, NA19117, HG03565, HG02971, HG03157, HG02970, NA19472, HG03025, NA20334, NA19713, NA19474, HG02107, NA19093, HG03060, NA19185, NA19116, HG03077, HG01914, HG01883, HG03162, NA19430, HG02861, NA18488, HG02851, HG02805, HG01886, HG03198, HG02808, HG03166, HG03265

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3603014

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	136
Observed Complex	0
Frequency	n/a