# |
Unit |
Min |
Off |
Def |
+/- |
W |
L |
Win% |
1 |
Rubio-Ridnour-Johnson-Love-Milicic |
136 |
.91 |
.93 |
-5 |
4 |
6 |
40 |
2 |
Ridnour-Johnson-Beasley-Love-Milicic |
104 |
1.00 |
1.08 |
-12 |
1 |
6 |
14 |
3 |
Ridnour-Ellington-Johnson-Love-Milicic |
48 |
.89 |
1.20 |
-26 |
1 |
3 |
25 |
4 |
Barea-Webster-Williams-Beasley-Milicic |
33 |
1.37 |
1.00 |
19 |
2 |
2 |
50 |
5 |
Rubio-Ellington-Williams-Love-Milicic |
29 |
1.10 |
1.04 |
7 |
2 |
1 |
66 |
6 |
Rubio-Ridnour-Williams-Love-Milicic |
15 |
.84 |
.78 |
2 |
1 |
0 |
100 |
7 |
Rubio-Ellington-Beasley-Love-Milicic |
8 |
.83 |
.94 |
0 |
1 |
2 |
33 |
8 |
Ridnour-Ellington-Beasley-Randolph-Milicic |
7 |
.93 |
.92 |
1 |
1 |
0 |
100 |
9 |
Ridnour-Webster-Johnson-Love-Milicic |
6 |
.79 |
.79 |
0 |
0 |
0 |
0 |
10 |
Ridnour-Ellington-Tolliver-Love-Milicic |
6 |
1.25 |
1.64 |
-3 |
0 |
1 |
0 |
11 |
Barea-Ridnour-Beasley-Love-Milicic |
5 |
1.21 |
.62 |
9 |
3 |
0 |
100 |
12 |
Barea-Rubio-Tolliver-Williams-Milicic |
5 |
1.00 |
.82 |
1 |
1 |
1 |
50 |
13 |
Rubio-Ridnour-Beasley-Love-Milicic |
5 |
1.10 |
1.18 |
-2 |
1 |
2 |
33 |
14 |
Ridnour-Webster-Williams-Beasley-Milicic |
5 |
.70 |
1.50 |
-8 |
0 |
1 |
0 |
15 |
Barea-Ellington-Williams-Beasley-Milicic |
3 |
.63 |
1.25 |
-5 |
0 |
1 |
0 |
16 |
Rubio-Webster-Williams-Beasley-Milicic |
3 |
1.14 |
.78 |
1 |
1 |
0 |
100 |
17 |
Barea-Rubio-Johnson-Tolliver-Milicic |
3 |
1.25 |
1.43 |
0 |
0 |
0 |
0 |
18 |
Rubio-Ridnour-Ellington-Love-Milicic |
3 |
.67 |
1.00 |
-3 |
0 |
1 |
0 |
19 |
Barea-Ridnour-Johnson-Love-Milicic |
3 |
1.57 |
.86 |
5 |
2 |
0 |
100 |
20 |
Barea-Rubio-Webster-Williams-Milicic |
3 |
.33 |
1.29 |
-7 |
0 |
1 |
0 |
# |
Unit |
eFG |
eFGA |
FTA |
Close |
dClose |
Reb |
T/O |
1 |
Rubio-Ridnour-Johnson-Love-Milicic |
.370 |
.424 |
+3 |
32% |
28% |
48% |
+1% |
2 |
Ridnour-Johnson-Beasley-Love-Milicic |
.437 |
.451 |
+6 |
33% |
27% |
56% |
-12% |
3 |
Ridnour-Ellington-Johnson-Love-Milicic |
.387 |
.512 |
+3 |
40% |
21% |
50% |
-8% |
4 |
Barea-Webster-Williams-Beasley-Milicic |
.622 |
.410 |
+7 |
29% |
28% |
48% |
-7% |
5 |
Rubio-Ellington-Williams-Love-Milicic |
.451 |
.453 |
+12 |
33% |
28% |
47% |
+4% |
6 |
Rubio-Ridnour-Williams-Love-Milicic |
.333 |
.391 |
0 |
43% |
26% |
53% |
+16% |
7 |
Rubio-Ellington-Beasley-Love-Milicic |
.500 |
.467 |
+5 |
50% |
33% |
54% |
-20% |
8 |
Ridnour-Ellington-Beasley-Randolph-Milicic |
.500 |
.357 |
+2 |
33% |
36% |
53% |
-14% |
9 |
Ridnour-Webster-Johnson-Love-Milicic |
.417 |
.385 |
+1 |
42% |
54% |
45% |
0% |
10 |
Ridnour-Ellington-Tolliver-Love-Milicic |
.545 |
.750 |
+2 |
45% |
50% |
42% |
+10% |
11 |
Barea-Ridnour-Beasley-Love-Milicic |
.462 |
.571 |
+4 |
31% |
43% |
49% |
+46% |
12 |
Barea-Rubio-Tolliver-Williams-Milicic |
.500 |
.222 |
+1 |
33% |
22% |
49% |
-11% |
13 |
Rubio-Ridnour-Beasley-Love-Milicic |
.364 |
.333 |
-5 |
36% |
0% |
71% |
+8% |
14 |
Ridnour-Webster-Williams-Beasley-Milicic |
.375 |
.545 |
-2 |
13% |
55% |
33% |
-10% |
15 |
Barea-Ellington-Williams-Beasley-Milicic |
.250 |
.500 |
-3 |
25% |
17% |
58% |
-12% |
16 |
Rubio-Webster-Williams-Beasley-Milicic |
.500 |
.429 |
-1 |
17% |
14% |
50% |
0% |
17 |
Barea-Rubio-Johnson-Tolliver-Milicic |
.600 |
.500 |
+2 |
20% |
60% |
10% |
-11% |
18 |
Rubio-Ridnour-Ellington-Love-Milicic |
.250 |
.500 |
-6 |
38% |
0% |
67% |
+28% |
19 |
Barea-Ridnour-Johnson-Love-Milicic |
.750 |
.429 |
+4 |
25% |
43% |
40% |
0% |
20 |
Barea-Rubio-Webster-Williams-Milicic |
.143 |
.667 |
-1 |
29% |
17% |
67% |
-2% |