Variant Details

Variant: esv3627284

Internal ID

7014114

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:93201602..93205578	hg38	UCSC Ensembl
Inner	chr11:93201602..93205578	hg38	UCSC Ensembl
Outer	chr11:93201387..93205834	hg38	UCSC Ensembl
	chr11:92934768..92938744	hg19	UCSC Ensembl
Inner	chr11:92934768..92938744	hg19	UCSC Ensembl
Outer	chr11:92934553..92939000	hg19	UCSC Ensembl

Cytoband

11q21

Allele length

Assembly	Allele length
hg38	3977
hg19	3977

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv14236413, essv14236382, essv14236385, essv14236406, essv14236425, essv14236445, essv14236386, essv14236396, essv14236376, essv14236438, essv14236439, essv14236430, essv14236426, essv14236423, essv14236404, essv14236429, essv14236403, essv14236389, essv14236372, essv14236446, essv14236366, essv14236427, essv14236417, essv14236377, essv14236381, essv14236444, essv14236379, essv14236393, essv14236407, essv14236370, essv14236435, essv14236411, essv14236440, essv14236375, essv14236434, essv14236420, essv14236398, essv14236422, essv14236424, essv14236391, essv14236390, essv14236388, essv14236432, essv14236414, essv14236409, essv14236437, essv14236401, essv14236367, essv14236371, essv14236408, essv14236441, essv14236383, essv14236418, essv14236443, essv14236400, essv14236433, essv14236397, essv14236395, essv14236436, essv14236405, essv14236402, essv14236394, essv14236416, essv14236399, essv14236428, essv14236421, essv14236384, essv14236442, essv14236387, essv14236380, essv14236368, essv14236369, essv14236419, essv14236378, essv14236374, essv14236392, essv14236415, essv14236410, essv14236431, essv14236412, essv14236373

Samples

NA20874, NA21097, HG01054, NA20783, NA21100, HG04076, NA20298, NA20332, HG00737, NA20798, NA19762, HG01177, HG01676, NA20586, NA20774, HG00330, HG03736, HG01710, HG04182, HG01761, HG00346, NA12275, NA12005, HG03910, HG01398, HG03968, HG02597, HG01440, HG01048, HG01058, HG01605, HG01550, NA20755, NA20753, HG01942, HG00149, NA20892, HG03787, HG01104, NA20505, HG02236, NA12872, HG01095, HG04195, HG03636, HG01142, NA20832, HG00740, NA21141, NA20859, HG01197, NA21112, NA06989, NA19752, HG02601, HG01589, NA20765, HG03934, HG00254, NA11881, HG02223, HG03708, NA20804, HG02651, HG01933, NA21094, NA20887, HG02401, HG00342, HG01055, NA20510, NA20826, HG01431, NA11892, NA20908, HG03686, HG01695, HG01061, HG01618, HG01516, HG03741

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3627284

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	81
Observed Complex	0
Frequency	n/a