Variant Details

Variant: esv3635717

Internal ID

7022515

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr15:19800619..19807270	hg38	UCSC Ensembl
Inner	chr15:19800769..19807120	hg38	UCSC Ensembl
Outer	chr15:19800469..19807420	hg38	UCSC Ensembl
	chr15:20005872..20012523	hg19	UCSC Ensembl
Inner	chr15:20006022..20012373	hg19	UCSC Ensembl
Outer	chr15:20005722..20012673	hg19	UCSC Ensembl

Cytoband

15q11.1

Allele length

Assembly	Allele length
hg38	6652
hg19	6652

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv15137483, essv15137506, essv15137529, essv15137553, essv15137533, essv15137540, essv15137490, essv15137547, essv15137512, essv15137576, essv15137521, essv15137554, essv15137501, essv15137494, essv15137497, essv15137539, essv15137570, essv15137524, essv15137555, essv15137519, essv15137549, essv15137574, essv15137487, essv15137488, essv15137561, essv15137498, essv15137568, essv15137551, essv15137495, essv15137572, essv15137559, essv15137567, essv15137542, essv15137575, essv15137493, essv15137511, essv15137516, essv15137515, essv15137552, essv15137534, essv15137492, essv15137525, essv15137527, essv15137503, essv15137538, essv15137526, essv15137560, essv15137514, essv15137544, essv15137563, essv15137482, essv15137531, essv15137484, essv15137566, essv15137513, essv15137509, essv15137565, essv15137577, essv15137518, essv15137486, essv15137496, essv15137550, essv15137502, essv15137500, essv15137536, essv15137510, essv15137505, essv15137520, essv15137528, essv15137522, essv15137485, essv15137571, essv15137541, essv15137499, essv15137569, essv15137546, essv15137523, essv15137557, essv15137556, essv15137489, essv15137562, essv15137543, essv15137573, essv15137564, essv15137507, essv15137530, essv15137558, essv15137545, essv15137508, essv15137537, essv15137535, essv15137532, essv15137517, essv15137548, essv15137491, essv15137504

Samples

HG00114, HG02339, HG00235, NA21110, NA19028, HG03800, HG00142, HG03731, HG00242, HG00351, HG00358, NA18507, NA18881, NA18979, HG00306, NA18639, HG03130, NA18878, HG00150, HG03069, NA18962, HG00272, HG02105, HG02087, HG01488, HG02620, NA19457, NA19088, HG00355, HG00369, NA21103, NA18498, HG03479, HG00311, NA19404, HG03268, HG01628, NA18977, NA18868, NA19238, HG00182, NA19036, NA20845, HG02104, NA19239, HG01275, NA18867, NA19921, HG02819, HG01699, NA19908, HG03160, HG03132, HG03511, HG02334, HG02090, HG01344, HG03928, NA18939, HG03491, NA12718, HG01345, HG02497, HG04177, NA18757, NA19118, HG03951, HG00350, NA19452, HG02256, NA19225, HG02484, NA21117, HG02282, HG00265, HG03437, NA19019, HG02546, HG02088, HG00366, HG02220, HG01272, NA19380, NA18992, HG02982, NA19741, HG02317, NA19818, NA19117, HG03600, NA18994, HG02113, NA19185, HG00595, HG02805, HG01097

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3635717

Frequency

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