The effect of varying the fraction of charged monomer units of the polyion in aqueous polyion-oppositely charged surfactant complex salts has been investigated. The complex salts used were based on cetyltrimethylammonium (C(16)TA(+)) with three different polymeric counterions: poly(acrylate) (PA(-)) or poly(acrylate) copolymerized with either dimethylacrylamide (PA(-)/DAM) or N-isopropylamide (PA(-)/NIPAM). The charge density of the polyion was varied by either adding poly(acrylic) acid (PAA) to the C(16)TAPA complex salt (annealed charges) or by varying the fraction of uncharged units in the C(16)TAPA/DAM or C(16)TAPA/NIPAM complex salts (quenched charges). The formed phases were studied visually between crossed polarizers and by small angle X-ray scattering (SAXS). Both types of complex salts (annealed and quenched) formed hexagonal phases at high fractions of charged monomers and low water contents. Upon increasing the water content, a cubic phase of the Pm3n space group was found. Upon further addition of water, a miscibility gap with the cubic phase in equilibrium with pure water was found. Decreasing the fraction of charged monomers in the annealed complex salt resulted in an increase of the curvature of the surfactant aggregates. Only at very low (< 0.05) fractions of charged monomers did the packing of the surfactant aggregates lose long-range order, and eventually, the miscibility gap disappeared. For the quenched complex salts, the changes upon decreasing the fraction of charged monomers in the polyion were similar, but the loss of long-range order occurred at much higher fractions of charged monomers. The average surfactant aggregation number in the surfactant aggregates, which was similar for the annealed and quenched systems, decreased when the fraction of charged monomers was decreased.