Your daughter is guaranteed to at least be a carrier, since you had no 'normal' cftr gene to pass on to her. It's just a matter now of whether or not her father passed on a mutation.
Her test will show 3819+10kbc>t <b>or</b> r668C from you, and either nothing else <b>or</b> a 2nd mutation from her father. She should make sure she has the Ambry Amplified with deletions/duplications.