Variant CNV_M1_HG19_17_33681421_33739337
Location: chr17:33681421-33739337 (57Kb)
Site classification: Deletion
Variant DCN frequency: 0.004
Genes Overlapped
Site classification: Deletion
Variant DCN frequency: 0.004
Genes Overlapped
| SLFN11 | CDS | schlafen family member 11 |
| SLFN12 | CDS | schlafen family member 12 |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2
ASW 0 0 45
CEU 0 1 65
CHB 0 0 78
CHS 0 0 91
CLM 0 0 49
FIN 0 2 60
GBR 0 0 54
IBS 0 0 6
JPT 0 0 69
LWK 0 0 69
MXL 0 0 54
PUR 0 0 52
TSI 0 0 83
YRI 0 0 71
AFR 0 0 140
AFR+ 0 0 185
AMR 0 0 155
ASN 0 0 238
EUR 0 3 268
ALL 0 3 846
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2
ASW 0 0 45
CEU 0 1 65
CHB 0 0 78
CHS 0 0 91
CLM 0 0 49
FIN 0 2 60
GBR 0 0 54
IBS 0 0 6
JPT 0 0 69
LWK 0 0 69
MXL 0 0 54
PUR 0 0 52
TSI 0 0 83
YRI 0 0 71
AFR 0 0 140
AFR+ 0 0 185
AMR 0 0 155
ASN 0 0 238
EUR 0 3 268
ALL 0 3 846
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI