| C |
|
|
 |
 |
@Phi |
L, 2-1 |
12% |
0.2 |
0.1 |
-0.2 |
0.5 |
0.0 |
0.0 |
1.6 |
9.2 |
0.0 |
0.0 |
| C |
|
|
 |
 |
@Phi |
L, 2-1 |
21% |
0.2 |
0.5 |
0.1 |
0.5 |
0.1 |
0.0 |
1.7 |
7.0 |
0.0 |
0.0 |
| C |
|
|
 |
 |
@Phi |
L, 2-1 |
0% |
0.0 |
0.1 |
0.0 |
0.2 |
0.0 |
0.0 |
0.2 |
0.0 |
0.0 |
0.0 |
| LW |
|
|
 |
 |
|
|
86% |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
| LW |
|
|
 |
 |
@Phi |
L, 2-1 |
79% |
0.3 |
0.5 |
0.0 |
0.6 |
0.3 |
0.0 |
1.8 |
4.5 |
0.0 |
0.0 |
| LW |
|
|
 |
 |
Nsh |
W, 6-3 |
25% |
0.4 |
0.6 |
-0.1 |
0.4 |
0.4 |
0.0 |
1.1 |
1.8 |
0.0 |
0.0 |
| RW |
|
|
 |
 |
@Phi |
L, 2-1 |
71% |
0.4 |
0.3 |
0.0 |
2.1 |
0.2 |
0.0 |
2.4 |
0.7 |
0.0 |
0.0 |
| RW |
|
|
 |
 |
@Phi |
L, 2-1 |
1% |
0.1 |
0.1 |
0.1 |
0.7 |
0.0 |
0.0 |
1.0 |
2.3 |
0.0 |
0.0 |
| RW |
|
|
 |
 |
|
|
2% |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
| D |
|
|
 |
 |
|
|
52% |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
| D |
|
|
 |
 |
|
|
29% |
0.3 |
0.5 |
0.0 |
0.3 |
0.2 |
0.0 |
1.6 |
0.0 |
0.0 |
0.0 |
| D |
|
|
 |
 |
NJ |
W, 2-1 |
0% |
0.0 |
0.0 |
0.0 |
0.1 |
0.0 |
0.0 |
0.2 |
0.0 |
0.0 |
0.0 |
| D |
|
|
 |
 |
|
|
32% |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
| D |
|
|
 |
 |
|
|
1% |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
| BN |
|
|
 |
 |
@Phi |
L, 2-1 |
0% |
0.1 |
0.2 |
0.0 |
2.3 |
0.0 |
0.0 |
1.0 |
1.6 |
0.0 |
0.0 |
| BN |
|
|
 |
 |
|
|
4% |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
| BN |
|
|
 |
 |
|
|
1% |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
| BN |
|
|
 |
 |
|
|
23% |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
| BN |
|
|
 |
 |
NJ |
W, 2-1 |
4% |
0.1 |
0.2 |
0.0 |
0.1 |
0.1 |
0.0 |
1.3 |
5.9 |
0.0 |
0.0 |