Variant CNV_M1_HG19_12_1074091_1078813
Location: chr12:1074091-1078813 (4.7Kb)
Site classification: Deletion
Variant DCN frequency: 0.006
Genes Overlapped
Site classification: Deletion
Variant DCN frequency: 0.006
Genes Overlapped
| RAD52 | INTRON | recombinase RAD52 |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2 CN3
ASW 0 1 44 0
CEU 0 0 66 0
CHB 0 0 78 0
CHS 0 0 91 0
CLM 0 0 48 1
FIN 0 0 62 0
GBR 0 0 54 0
IBS 0 0 6 0
JPT 0 0 69 0
LWK 0 2 67 0
MXL 0 0 54 0
PUR 0 0 52 0
TSI 0 0 83 0
YRI 0 2 69 0
AFR 0 4 136 0
AFR+ 0 5 180 0
AMR 0 0 154 1
ASN 0 0 238 0
EUR 0 0 271 0
ALL 0 5 843 1
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2
ASW 0 1 44
CEU 0 0 66
CHB 0 0 78
CHS 0 0 91
CLM 0 0 48
FIN 0 0 62
GBR 0 0 54
IBS 0 0 6
JPT 0 0 69
LWK 0 2 66
MXL 0 0 54
PUR 0 0 52
TSI 0 0 83
YRI 0 2 69
AFR 0 4 135
AFR+ 0 5 179
AMR 0 0 154
ASN 0 0 238
EUR 0 0 271
ALL 0 5 842
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI