Variant CNV_M1_HG19_5_34074353_34086793
Location: chr5:34074353-34086793 (12Kb)
Site classification: Deletion
Variant DCN frequency: 0.017
Genes Overlapped
Site classification: Deletion
Variant DCN frequency: 0.017
Genes Overlapped
| C1QTNF3 | INTRON | complement C1q tumor necrosis factor-related protein 3 isoform b precursor |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2
ASW 0 4 41
CEU 0 0 66
CHB 0 0 78
CHS 0 0 91
CLM 0 1 48
FIN 0 0 62
GBR 0 0 54
IBS 0 0 6
JPT 0 0 69
LWK 0 2 67
MXL 0 0 54
PUR 0 2 50
TSI 0 0 83
YRI 0 5 66
AFR 0 7 133
AFR+ 0 11 174
AMR 0 3 152
ASN 0 0 238
EUR 0 0 271
ALL 0 14 835
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2
ASW 0 4 41
CEU 0 0 66
CHB 0 0 78
CHS 0 0 91
CLM 0 1 48
FIN 0 0 61
GBR 0 0 54
IBS 0 0 6
JPT 0 0 69
LWK 0 2 67
MXL 0 0 54
PUR 0 2 50
TSI 0 0 83
YRI 0 5 66
AFR 0 7 133
AFR+ 0 11 174
AMR 0 3 152
ASN 0 0 238
EUR 0 0 270
ALL 0 14 834
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI