Consumer files sometimes carry mitochondrial variants that aren’t part of any currently named branch — they can be private or family-specific changes, or simply variants the published tree hasn’t formally named yet. We don’t assign you to a branch these might imply, because doing so without confirmation would be guessing. They’re noted, not used to over-call your result.
My file has extra variants that don’t match any named branch — what are those?
What unnamed mitochondrial variants in your file are, and why we note them rather than use them to over-call your result.