I'm still not sure what you're asking or saying. Damn. I'll try to answer and hope I hit the right general area.
Utilities like Whit Athey's predictor look at the STR pattern (the markers, and the number of times the pattern repeats at each location). It's not uncommon to find exact matches between unrelated men on a bunch of different markers. But, it would be amazing if two different men had 24 matching or closely matching markers and not be in the same haplogroup.
It does happen, though. Particularly in haplogroup R1b where the group is so old and so large that the chance of convergence is much higher. I think I mentioned earlier that at 37 markers the algorithm couldn't tell if I'm I1 or G2a. At 67 markers it's (now) clear that I'm almost certainly G2a. But it's a moot point because I've already tested and been found positive for the SNPs that define G2a.
When the predictor says there is 100 percent probability that your markers are I1, then you are an easy case. You probably see some other percentages for other haplogroups. Maybe 15 percent change you are G2a, or a 10 percent chance you are R1. (Just making up numbers here for the purpose of illustration.)
If you're seeing something like that, it's not a mistake. It would mean your pattern of STR markers really does match I1 perfectly but it isn't proof. There are miscellaneous probabilities that you could actually belong to one of those haplogroups. You are "close enough" there is some chance, even if it's not very high. That's because DNA testing is on-going. New data is always coming in. There is no way to know absolutely and for sure what the upper and lower limits are for the markers in every haplogroup.