Variant Details

Variant: esv3625898

Internal ID

7012732

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:33848531..33851312	hg38	UCSC Ensembl
Inner	chr11:33848533..33851310	hg38	UCSC Ensembl
Outer	chr11:33848529..33851314	hg38	UCSC Ensembl
	chr11:33870077..33872858	hg19	UCSC Ensembl
Inner	chr11:33870079..33872856	hg19	UCSC Ensembl
Outer	chr11:33870075..33872860	hg19	UCSC Ensembl

Cytoband

11p13

Allele length

Assembly	Allele length
hg38	2782
hg19	2782

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv14088466, essv14088509, essv14088492, essv14088460, essv14088472, essv14088507, essv14088434, essv14088455, essv14088533, essv14088457, essv14088524, essv14088508, essv14088458, essv14088523, essv14088476, essv14088482, essv14088514, essv14088479, essv14088497, essv14088540, essv14088541, essv14088529, essv14088489, essv14088510, essv14088519, essv14088442, essv14088484, essv14088501, essv14088495, essv14088503, essv14088490, essv14088504, essv14088526, essv14088531, essv14088483, essv14088477, essv14088444, essv14088521, essv14088486, essv14088462, essv14088496, essv14088485, essv14088539, essv14088537, essv14088518, essv14088438, essv14088459, essv14088491, essv14088528, essv14088475, essv14088478, essv14088502, essv14088439, essv14088516, essv14088520, essv14088499, essv14088517, essv14088454, essv14088433, essv14088542, essv14088443, essv14088440, essv14088437, essv14088511, essv14088469, essv14088505, essv14088447, essv14088538, essv14088470, essv14088487, essv14088480, essv14088527, essv14088474, essv14088493, essv14088446, essv14088532, essv14088463, essv14088544, essv14088534, essv14088435, essv14088441, essv14088530, essv14088456, essv14088449, essv14088488, essv14088461, essv14088506, essv14088543, essv14088525, essv14088448, essv14088450, essv14088453, essv14088522, essv14088451, essv14088465, essv14088468, essv14088513, essv14088515, essv14088464, essv14088500, essv14088535, essv14088471, essv14088473, essv14088545, essv14088445, essv14088481, essv14088452, essv14088512, essv14088494, essv14088467, essv14088536, essv14088436, essv14088498

Samples

NA18745, HG00881, NA19058, HG00592, NA19066, HG00559, HG02026, HG02035, NA18561, HG02029, NA18599, NA18603, HG00729, HG01806, NA19355, HG01486, NA18596, HG02382, NA18625, HG00449, HG02384, NA19314, NA18602, NA18627, HG00663, NA19076, HG02156, HG00674, NA18635, HG02521, NA18993, NA18558, NA18547, HG00634, NA18618, HG02130, HG02085, HG00851, NA19088, NA18964, HG01859, HG00590, HG02067, HG01849, NA18748, NA18617, HG00422, NA19471, NA18966, HG02190, NA18990, NA18557, NA18954, HG02164, HG02134, NA18614, HG02047, NA18605, NA19657, HG00443, NA19082, HG03714, NA18525, HG02075, HG00557, HG02397, NA19391, NA18991, HG01938, HG00475, HG00556, HG00598, NA18579, NA18981, HG00708, NA19064, NA18566, HG00651, NA19084, HG00956, NA18946, HG01921, HG01842, HG02081, HG02184, NA18963, HG02031, HG00864, NA18541, NA18953, HG00407, NA19003, NA18559, HG01980, NA19434, NA18629, NA18943, HG02019, NA19376, HG00672, HG00614, HG00513, NA18631, HG01804, NA19060, HG00698, NA18983, NA19004, HG01869, HG01927, HG00437, HG02060, NA18965

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3625898

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	113
Observed Complex	0
Frequency	n/a