Variant Details

Variant: esv3641259

Internal ID

7028033

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr17:75111618..75112178	hg38	UCSC Ensembl
Inner	chr17:75111621..75112176	hg38	UCSC Ensembl
Outer	chr17:75111616..75112181	hg38	UCSC Ensembl
	chr17:73107713..73108273	hg19	UCSC Ensembl
Inner	chr17:73107716..73108271	hg19	UCSC Ensembl
Outer	chr17:73107711..73108276	hg19	UCSC Ensembl

Cytoband

17q25.1

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

essv15740613, essv15740595, essv15740577, essv15740601, essv15740584, essv15740570, essv15740533, essv15740599, essv15740589, essv15740598, essv15740594, essv15740543, essv15740585, essv15740540, essv15740550, essv15740532, essv15740576, essv15740535, essv15740614, essv15740586, essv15740527, essv15740581, essv15740567, essv15740569, essv15740560, essv15740537, essv15740604, essv15740596, essv15740561, essv15740600, essv15740536, essv15740548, essv15740547, essv15740592, essv15740526, essv15740562, essv15740611, essv15740616, essv15740617, essv15740583, essv15740573, essv15740580, essv15740578, essv15740546, essv15740606, essv15740565, essv15740610, essv15740552, essv15740572, essv15740531, essv15740620, essv15740619, essv15740566, essv15740574, essv15740618, essv15740582, essv15740564, essv15740563, essv15740528, essv15740607, essv15740529, essv15740557, essv15740544, essv15740587, essv15740549, essv15740545, essv15740538, essv15740556, essv15740588, essv15740553, essv15740541, essv15740590, essv15740575, essv15740608, essv15740597, essv15740539, essv15740593, essv15740542, essv15740615, essv15740603, essv15740579, essv15740571, essv15740605, essv15740568, essv15740554, essv15740559, essv15740558, essv15740530, essv15740612, essv15740609, essv15740621, essv15740534, essv15740591, essv15740602, essv15740551, essv15740555

Samples

HG02614, HG01985, NA18502, HG03096, HG01413, NA19222, HG01885, HG02337, HG03449, HG00640, NA19092, NA20294, NA19355, HG03455, HG01486, NA19777, HG03126, HG03297, HG02888, NA19098, HG01051, HG03074, NA19201, HG02810, HG03452, NA19307, HG02325, HG02840, NA19131, NA19197, NA19138, HG02922, HG02489, HG03556, HG02315, HG03195, HG02588, NA19159, HG03225, HG02946, NA19239, NA19209, HG03055, HG02716, HG03120, HG03054, HG03088, NA19175, NA19462, HG02108, HG02554, HG01989, HG01142, HG01345, HG02508, HG03124, NA19461, NA19118, HG02817, NA18499, HG03078, HG03391, HG02979, NA19257, HG03046, HG02585, HG03354, NA19160, HG02586, HG02594, HG03567, HG02255, HG01363, HG02613, HG03028, HG02807, HG02667, HG03240, NA19149, HG02759, HG02546, HG01396, NA19144, HG01375, HG02771, NA19248, HG03279, HG03063, NA19102, HG01883, HG02763, HG02861, NA19316, HG02643, NA19153, HG03166

Known Genes

ARMC7

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3641259

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	96
Observed Complex	0
Frequency	n/a