|
Whole genome
|
p term (7 MB)b
|
Mid-chromosome
|
q term decilesc
|
---|
Haseman-Elston
|
mean
|
0.503
|
0.502
|
0.503
|
0.506
|
SD
|
0.018
|
0.035
|
0.019
|
0.037
|
No. SNPsa
|
9857–10803
|
383–437
|
9059–9968
|
330–386
|
ROMP-one
|
mean
|
0.496
|
0.494
|
0.496
|
0.498
|
SD
|
0.015
|
0.023
|
0.015
|
0.020
|
No. SNPsa
|
9817–10802
|
380–436
|
9023–9968
|
330–386
|
ROMP/ROOP-one
|
mean
|
0.487
|
0.485
|
0.487
|
0.488
|
SD
|
0.021
|
0.028
|
0.021
|
0.026
|
No. SNPsa
|
9769–10802
|
380–436
|
9016–9968
|
330–386
|
ROMP-all
|
mean
|
0.479
|
0.479
|
0.478
|
0.483
|
SD
|
0.032
|
0.035
|
0.032
|
0.034
|
No. SNPsa
|
9845–10807
|
381–437
|
9051–9972
|
330–386
|
ROMP/ROOP-all
|
mean
|
0.456
|
0.453
|
0.456
|
0.459
|
SD
|
0.034
|
0.042
|
0.034
|
0.035
|
No. SNPsa
|
9825–10807
|
381–437
|
9030–9972
|
330–386
|
- aThe number of SNPs varies due to missing data and variable numbers of markers excluded by synteny.
- bThe p ends of chromosomes 13, 14, 15, 19, 21, 22 could not be used.
- cThe q ends of chromosomes 9, 16, 17 could not be used.