An unusual hexagonal dot pattern has been observed in thin films of symmetric diblock copolymers experimentally. In order to verify the stability of the hexagonal dot pattern and understand its formation mechanism, we investigate the self-assembly of AB diblock copolymers in ultrathin films with a neutral top surface and a B-selective bottom surface using self-consistent field theory (SCFT) and dissipative particle dynamics (DPD). Our SCFT results reveal that ideally symmetric diblock copolymers with A-block volume fraction f = 0.5 can indeed form a hexagonal dot pattern in a certain range of film thickness (h), which is actually a half-period perforated lamellar (hPL A ) morphology. The hPL A morphology transfers to a patternless half-period parallel lamella (hL ∥ ) with increasing h and to a stripe pattern (L ⊥ ) with decreasing h. The phase diagram with respect to f and h further demonstrates that the stable region of hPL A shifts to small f as h increases and disappears at a critical value of h. The formation of the hPL A region is mainly caused by the competition between the A/B interfacial energy and the overall surface energy (including top and bottom). In addition, the formation of hPL A is also verified by DPD simulations. Therefore, our work confirms that the experimentally observed dot pattern in thin films of symmetric diblock copolymers is an equilibrium morphology, the formation of which requires ultrathin thickness and asymmetric surface affinities.