Variant Details

Variant: esv3641299

Internal ID

7028073

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr17:76790360..76794892	hg38	UCSC Ensembl
Inner	chr17:76790860..76794392	hg38	UCSC Ensembl
Outer	chr17:76789360..76795892	hg38	UCSC Ensembl
	chr17:74786442..74790974	hg19	UCSC Ensembl
Inner	chr17:74786942..74790474	hg19	UCSC Ensembl
Outer	chr17:74785442..74791974	hg19	UCSC Ensembl

Cytoband

17q25.1

Allele length

Assembly	Allele length
hg38	4533
hg19	4533

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv15745609, essv15745679, essv15745621, essv15745649, essv15745600, essv15745691, essv15745683, essv15745612, essv15745689, essv15745674, essv15745646, essv15745608, essv15745607, essv15745601, essv15745638, essv15745604, essv15745611, essv15745694, essv15745678, essv15745615, essv15745673, essv15745630, essv15745686, essv15745690, essv15745650, essv15745660, essv15745626, essv15745651, essv15745657, essv15745666, essv15745647, essv15745613, essv15745688, essv15745682, essv15745669, essv15745627, essv15745610, essv15745614, essv15745616, essv15745671, essv15745667, essv15745628, essv15745670, essv15745681, essv15745668, essv15745677, essv15745641, essv15745685, essv15745655, essv15745618, essv15745661, essv15745631, essv15745634, essv15745632, essv15745664, essv15745643, essv15745636, essv15745603, essv15745606, essv15745652, essv15745642, essv15745692, essv15745639, essv15745654, essv15745619, essv15745620, essv15745659, essv15745629, essv15745625, essv15745662, essv15745622, essv15745658, essv15745605, essv15745672, essv15745684, essv15745645, essv15745617, essv15745648, essv15745624, essv15745693, essv15745602, essv15745633, essv15745687, essv15745675, essv15745656, essv15745653, essv15745663, essv15745680, essv15745623, essv15745676, essv15745637, essv15745635, essv15745640, essv15745644, essv15745665

Samples

HG02614, HG02610, HG02496, HG03121, NA18881, HG03449, NA18917, NA19350, HG03521, HG03455, HG03100, HG02624, NA20332, HG03172, NA19443, NA18870, NA20771, HG03436, HG03086, NA19315, HG03452, NA19198, NA18916, HG03105, HG02816, HG03079, HG02281, HG02562, NA12005, HG02573, HG03045, HG01369, NA19235, NA19026, HG02571, NA18520, HG02946, HG01198, NA20342, HG02009, HG03120, NA20535, NA19908, HG03160, HG03132, HG03511, NA19984, HG02511, HG01882, HG02108, HG03457, NA18915, HG01989, HG03159, HG02470, HG01889, HG02577, HG03078, NA18853, HG02666, HG01890, HG02635, HG02586, HG03109, HG02772, HG01363, HG02455, HG02807, HG03461, NA19147, HG02546, NA19435, NA19439, HG02317, HG03557, HG02558, HG03084, NA20357, NA18501, HG02971, HG03112, NA19438, NA19351, HG02646, HG03351, HG03410, NA18876, NA19116, HG03077, HG03538, HG03162, HG02805, NA19463, NA18511, NA19429

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3641299

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	95
Observed Complex	0
Frequency	n/a