Variant CNV_M1_HG19_11_107783714_107788257
Location: chr11:107783714-107788257 (4.5Kb)
Site classification: Deletion
Variant DCN frequency: 0.342
Genes Overlapped
Site classification: Deletion
Variant DCN frequency: 0.342
Genes Overlapped
| SLC35F2 | INTRON | solute carrier family 35 member F2 |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2
ASW 2 8 35
CEU 1 22 43
CHB 5 37 36
CHS 10 32 49
CLM 2 18 29
FIN 2 16 44
GBR 2 11 41
IBS 1 2 3
JPT 3 26 40
LWK 1 19 49
MXL 0 8 46
PUR 1 14 37
TSI 5 27 51
YRI 2 16 53
AFR 3 35 102
AFR+ 5 43 137
AMR 3 40 112
ASN 18 95 125
EUR 11 78 182
ALL 37 256 556
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2
ASW 2 8 35
CEU 1 22 43
CHB 5 37 36
CHS 10 31 48
CLM 2 16 29
FIN 2 16 44
GBR 2 11 41
IBS 1 2 3
JPT 3 26 40
LWK 1 18 49
MXL 0 8 46
PUR 1 14 37
TSI 5 27 51
YRI 2 16 53
AFR 3 34 102
AFR+ 5 42 137
AMR 3 38 112
ASN 18 94 124
EUR 11 78 182
ALL 37 252 555
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI